Effect of voice characteristics on the attended and unattended processing of two concurrent messages

Three experiments using dichotic listening measured the priming effect produced on the detection of a semantically defined target word in an attended list of words by a lexically identical word presented to the opposite ear with an attenuation of 12 dB. Experiment 1 embedded the prime in unattended continuous speech and found a 21 ms priming effect, but only when the voices of the two messages had different pitch ranges. Experiment 2 emphasised and generalised the priming effect to a more natural situation using voices differing both in pitch and timbre. This priming effect did not vary with word frequency. In Experiment 3 the prime was part of a list of isolated words played to the unattended ear. It found a 94 ms priming effect when there was no pitch-range difference between the two messages. This priming effect was larger for high-frequency words than for low. These results extend recent findings by Rivenez, Darwin, and Guillaume (2006) and demonstrate the importance of factors that influence perceptual organisation in determining the extent to which unattended messages can be processed.     

Stimulus–response translation in manual and vocal modality: Is age‐related slowing influenced by changes in working memory functioning?

In some conditions, age‐related slowing rates are higher for manual than for vocal responses. The interaction between age and response modality was examined in four experiments in which the performance of younger (M = 22.6 years) and older (M = 70.8 years) adults was compared under various stimulus–response mapping rules. The interaction effect was not observed in a simple localisation task on which the manual modality had an advantage in both age groups (Experiment 1). When congruence between stimulus and response was reduced (Experiment 2), manual responses were disproportionately slowed in older participants. In conceptual and size comparison tasks (Experiment 3), the age‐by‐modality effect was not influenced by working memory load during the interval between the first and the second stimulus presentation. In an identification task, age‐related slowing effects were less when responses were spoken names than when nonwords were used as labels (Experiment 4). These results indicate that older participants experience a specific difficulty in activating arbitrary S–R mapping rules during executive control.     

Default-mode network functional connectivity in aphasia: Therapy-induced neuroplasticity

Previous research on participants with aphasia has mainly been based on standard functional neuroimaging analysis. Recent studies have shown that functional connectivity analysis can detect compensatory activity, not revealed by standard analysis. Little is known, however, about the default-mode network in aphasia. In the current study, we studied changes in the default-mode network in subjects with aphasia who underwent semantic feature analysis therapy. We studied nine participants with chronic aphasia and compared them to 10 control participants. For the first time, we identified the default-mode network using spatial independent component analysis, in participants with aphasia. Intensive therapy improved integration in the posterior areas of the default-mode network concurrent with language improvement. Correlations between integration and improvement did not reach significance, but the trend suggests that pre-therapy integration of the default-mode network may predict therapy outcomes. Functional connectivity allows a better understanding of the impact of semantic feature analysis in aphasia.     

Impact of Motivational Climates on Claimed Self-Handicapping Strategies: Illustration in Tropical Environment

The purpose of the present study was to quantitatively and qualitatively examine whether claimed self-handicapping is increased in a performance motivational climate (PMC) compared with a mastery motivational climate (MMC) within a strictly controlled tropical environment. Participants completed measures of self-handicapping using open-ended questions before a physical test. The analyses revealed that (a) participants who engage in self-handicapping strategy were more numerous, (b) the number of self-handicap reported self-handicap score were greater, and (c) participants who engage in self-handicapping strategy reported more impediments in the PMC as compared with MMC. Information about the nature of self-handicapping claims is also provided.     

Children's memory distortions following social contact with a co-witness: Disentangling social and cognitive mechanisms

This study examined whether recalling an event with a co-witness influences children's recall. Individual 3-5-year-olds (n = 48) watched a film with a co-witness. Unbeknown to participants, the co-witness was watching an alternative version of the film. Afterwards both the co-witness and the participant answered questions about the film together (public recall), and the degree to which children conformed to the co-witness's alternative version of events was measured. Subsequently participants were questioned again individually (private recall). Children also completed false belief and inhibitory control tasks. By separating errors made in public and private, the results indicated that both social conformity (32% of errors) and memory distortion (68% of errors) played a role in co-witness influence. Inhibitory control predicted the likelihood of retracting errors in private, but only for children who failed (r=.66) rather than passed false belief tasks (r=-.10). The results suggest that children with a theory of mind conform in the company of the co-witness to avoid social embarrassment, while those a poor theory of mind conform on the basis of an inability to inhibit the co-witness's response. The findings contribute to our understanding of the motivations responsible for co-witness conformity across early childhood.     

Two-month-old infants of depressed mothers show mild, delayed and persistent change in emotional state after non-contingent interaction

The aim of this study was to explore how early infants show different responses to non-contingent maternal behavior according to their past history of relations with their mother. Two groups of 2-month-olds interacted with their mother who was assessed as depressed (group 1) or non-depressed (group 2). Although they received a continuous image and voice of their mothers, the infants were presented either a 30-s contingent maternal communication (live episode 1) or a thirty second non-contingent episode (replay of prior maternal communication), or again a 30-s contingent live episode (live2). The lower percentage of negative facial expressions displayed during replay by infants of depressed mothers suggests on one hand that they are less sensitive to a non-contingent maternal behavior than infants of non-depressed mothers. However, within group comparisons demonstrate a notable difference: while infants of non-depressed mothers show a U curve of smile, infants of depressed mothers show decreasing smile throughout the three episodes. Taken together, these results plead in favour of an other profile of sensitivity displayed by infants of depressed mothers. Instead of the strong but short-term reaction of infants of non-depressed mothers, the response of infants of depressed mothers appeared to be a mild, delayed and more persistent change in emotional state. These findings are discussed in the light of possible cognitive and social incidence of passive avoidance of stressful events in infants of depressed mothers.     

Hippocampal low-frequency stimulation and chronic mild stress similarly disrupt fear extinction memory in rats

Disruptions of fear extinction-related potentiation of synaptic efficacy in the connection between the hippocampus (HPC) and the medial prefrontal cortex (mPFC) have been shown to impair the recall of extinction memory. This study was undertaken to examine if chronic mild stress (CMS), which is known to alter induction of HPC–mPFC long-term potentiation, would also interfere with both extinction-related HPC–mPFC potentiation and extinction memory. Following fear conditioning (5 tone-shock pairings), rats were submitted to fear extinction (20 tone-alone presentations), which produced an increase in the amplitude of HPC–mPFC field potentials. HPC low-frequency stimulation (LFS), applied immediately after training, suppressed these changes and induced fear return during the retention test (5 tone-alone presentations). CMS, delivered before fear conditioning, did not interfere with fear extinction but blocked the development of extinction-related potentiation in the HPC–mPFC pathway and impaired the recall of extinction. These findings suggest that HPC LFS may provoke metaplastic changes in HPC outputs that may mimic alterations associated with a history of chronic stress.     

A kinematic and dynamic comparison of surface and underwater displacement in high level monofin swimming

Fin swimming performance can be divided into underwater and surface water races. World records are about 10% faster for underwater swimming vs. surface swimming, but little is known about the advantage of underwater swimming for monofin swimming. Some authors reported that the air–water interface influences the kinematics and leads to a narrow vertical amplitude of the fin. On the one hand, surface swimming is expected to affect drag parameters (cross-sectional area (S) and active drag (AD)) when compared to underwater swimming. On the other hand, the surface swimming technique may also affect efficiency (η_F). The aim of this study is therefore to evaluate and compare drag parameters and efficiency during underwater and surface swimming. To this end, 12 international level monofin swimmers were measured during both underwater and surface swimming. Kinematic parameters (both dimensional and non-dimensional), η_F (calculated according to the Elongated-Body Theory), and AD (computed with Velocity Perturbation Method) were calculated for an underwater and a surface fin swimming trial, performed at maximal speed. As expected, results showed significantly lower velocities during surface swimming vs. underwater  = 2.5 m s⁻¹ vs.  = 2.36 m s⁻¹, p < .01). Velocities during underwater and surface swimming were strongly correlated (r = .97, p < .01). Underwater swimming was also associated with higher vertical amplitudes of the fin compared to surface swimming ( = 0.55 m vs. ) = 0.46 m, p < .01). Length-specific amplitudes (A_under/L_b) were in the order of 20% during underwater swimming as for undulating fish, and significantly higher than during surface swimming (A_surf/L_b = 17%, p < .01). Efficiency for surface swimming was about 6% lower than for underwater swimming ( = 0.79 vs.  = 0.74, p < .01). This decrease could be associated with an increase in swimming frequency for surface swimming ( = 2.15 Hz vs.  = 2.08 Hz, p < .01). Active drag during surface swimming was about 7% higher than for underwater swimming ( = 78.9 N vs.  = 84.7 N, p < .01). A significantly smaller cross-sectional area for surface swimming ( = 0.053 m² vs.  = 0.044 m², p < .01) and higher drag coefficient for surface swimming ( = 0.47 vs.  = 0.69, p < .01) were measured. Finally, correlation between cross-sectional area and vertical amplitude of the fin was reported for both underwater and surface swimming. These results suggest that the performance improvement during underwater swimming is not only linked to a wave drag reduction effect but also to a specific swimming technique due to the free surface.     

How are Strouhal number, drag, and efficiency adjusted in high level underwater monofin-swimming?

Strouhal number (St) corresponds to a wake parameter based on the tail kinematics of swimming animals according to St=A.f/U, where f is the stroke frequency, A is the fin-beat peak-to-peak amplitude, and U is the forward speed. St number is a trade-off between amplitude and frequency that generates a forward velocity. This parameter may therefore be affected by swimming technique, which can be evaluated through active drag (AD) and Froude efficiency (eta(F)). The aim of our study was therefore to (1) investigate the range of AD and eta(F) values for high level monofin-swimmers, (2) explore the range of St numbers, and (3) examine to what extent this latter non-dimensional parameter may affect AD and eta(F). To this end, experiments have been conducted on 12 international level monofin-swimmers. St number, eta(F) (calculated according to the elongated-body theory), and AD (computed with velocity perturbation method) were calculated at the same time for an underwater fin-swimming trial, at maximal speed. Lowest values of St numbers (St=0.34) corresponded to fin-swimmers with highest velocities (R=-.77, p<.05), highest efficiencies (R=-.86, p<.001), and lowest active drag (R=.91, p<.001). On the one hand, AD was increased with vertical motion of the fin (R=.84, p<.001), which increased cross-sectional area (R=.78, p<.05). On the other hand, efficiencies showed a tendency to peak at eta(F)=0.82 in a narrow range of St numbers close to 0.4. This St range corresponded to the upper limit of the 0.25-0.4 range usually claimed for maximum efficiency of marine and flying animals. Such results suggest that increasing efficiency and reducing drag improves performance per se (regardless how these parameters are related with St number).